QC Manager

Site Name: Algeria - Boumerdes

Posted Date: Aug 2 2023

Purpose of the Position :

• Management of the Site Quality control.
• Implements the strategic action plan defined by the lead of the department.
• Plan and ensure the performance of the Quality Control activities.
• Ensures the marketing of compliant products of irreproachable quality in compliance with regulatory requirements and GSK Quality Standards (QMS,CAP).
• Respect of costs, deadlines, safety, and quality.
• Contribution to teamwork and the achievement of collective objectives.
• Continuous improvement in Quality Control activities.
  
  

Main responsibilities :

• Ensures the testing of finished products, materials, and packaging items within the required deadlines.
• Ensure the reliability of the physico-chemical and microbiological analytical data of pharmaceutical products as well as the testing data of packaging items by ensuring compliance with testing procedures.
• Ensures compliance with GMP, quality standards defined by GSK (QMS, CAP), pharmacopoeia, as well as local regulations in Quality Control.
• Training and continuous monitoring of technicians on effective testing methods and procedures provide the support needed to solve any technical problem.
• Contributes actively to the introduction of new products on the Site by identifying the human & equipment's needs and ensuring good organization in the Quality Control to meet the Site objectives.
• Ensures the achievement of analytical validations, analytical transfer, cleaning validation, as well as the testing needed for the validation process.
• Ensures the preparation, implementation, and follow-up) of internal GSK audits (GMP Audit, Independent Business Monitoring, Management Monitoring), ministry, and LNCPP with ensuring the implementation of corrective & preventive actions on time.
• Work on Quality Control activity continuous improvement by proposing an improvement plan (automation, simplification) and implementing the Lean Lab process.
• Establishes and monitors the performance indicators of Quality Control by identifying improvement actions to achieve the objectives of the department and the site.
• Identifies any GMP, quality, and safety problem, analyzes it, and implements the appropriate corrective actions.
  
  

Why you?

Basic Qualifications:

• BAC+5 or Master (Chemical Engineer, Microbiological DES, or Pharmacist).
• 5 years of experience in the laboratory.
  
  

Essential Skills and Abilities:

• Capable of working across boundaries and functional areas
• Familiarity/ experience with copy approval process
• Understands analytics and performance management
• Competent in working in multicultural environment
• Highly resilient, agile and is willing to stretch
• Ability to demonstrate excellence in execution and project management capabilities
• Organized and efficient worker
  
  

GSK is a global biopharma company with a special purpose – to unite science, technology and talent to get ahead of disease together – so we can positively impact the health of billions of people and deliver stronger, more sustainable shareholder returns – as an organisation where people can thrive. Getting ahead means preventing disease as well as treating it, and we aim to positively impact the health of 2.5 billion people by the end of 2030.

Our success absolutely depends on our people. While getting ahead of disease together is about our ambition for patients and shareholders, it’s also about making GSK a place where people can thrive. We want GSK to be a workplace where everyone can feel a sense of belonging and thrive as set out in our Equal and Inclusive Treatment of Employees policy. We’re committed to being more proactive at all levels so that our workforce reflects the communities we work and hire in, and our GSK leadership reflects our GSK workforce.

Contact information:

You may apply for this position online by selecting the Apply now button.

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